| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69437415-69437505 | Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:69643622-69643834 | Rare:78 | ||||
| chr2:69829517-69829737 | Common:1; Rare:87 | ||||
| chr2:69893887-69894017 | Rare:35 | ||||
| chr2:69914479-69914875 | Common:1; Rare:100 | ||||
| chr2:70086864-70087118 | Common:1; Rare:118 | ||||
| chr2:70087373-70087750 | Common:2; Rare:147 | ||||
| chr2:70087810-70087921 | Rare:25 | ||||
| chr2:70087933-70088363 | Common:1; Rare:111 | ||||
| chr2:70190971-70191150 | Common:1; Rare:47 | ||||
| chr2:70248468-70248793 | Common:4; Rare:132 | ||||
| chr2:70257901-70258167 | Common:1; Rare:83 | ||||
| chr2:70293378-70293504 | Rare:43 | ||||
| chr2:70293613-70293848 | Common:2; Rare:77 | ||||
| chr2:70767379-70767523 | Rare:46 |